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A8513

EHMT1 Rabbit polyclonal antibody

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£151.00

SKU:
A8513
Zusätzliche Namen:
EHMT1|EHMT1-IT1|Eu-HMTase1|EUHMTASE1|FP13812|GLP|GLP1|KLEFS1|KMT1D
Anwendung:
ELISA, WB
Molekulargewicht:
180kDa
Spezies-Reaktivität:
Human
Aufreinigung:
Affinity Purified
Lagerbedingungen:
-20[o]C Avoid freeze/thaw cycles.
Hersteller:
Abclonal
Host:
Rabbit
Reaktivitäten:
Human, Mouse, Rat
Immunogen:
Recombinant protein (or fragment).This information is considered to be commercially sensitive.
Formulierung:
Unmodified
Sequenz:
MAAADAEAVPARGEPQQDCCVKTELLGEETPMAADEGSAEKQAGEAHMAADGETNGSCENSDASSHANAAKHTQDSARVNPQDGTNTLTRIAENGVSERDSEAAKQNHVTADDFVQTSVIGSNGYILNKPALQAQPLRTTSTLASSLPGHAAKTLPGGAGKGRTPSAFPQTPAAPPATLGEGSADTEDRKLPAPGADVKVHRARKTMPKSVVGLHAASKDPREVREARDHKEPKEEINKNISDFGRQQLLPPFPSLHQSL
Uniprot:
Q9H9B1
Synonyme:
EHMT1 intronic transcript 1;EHMT1-IT1;Eu-HMTase1;euchromatic histone-lysine N-methyltransferase 1;EUHMTASE1;FP13812;G9a-like protein 1;GLP;GLP1;H3-K9-HMTase 5;histone H3-K9 methyltransferase 5;histone-lysine N-methyltransferase EHMT1;histone-lysine N-methyltransferase, H3 lysine-9 specific 5;KLEFS1;KMT1D;lysine N-methyltransferase 1D
Weitere Details:
The protein encoded by this gene is a histone methyltransferase that methylates the lysine-9 position of histone H3. This action marks the genomic region packaged with these methylated histones for transcriptional repression. This protein may be involved in the silencing of MYC- and E2F-responsive genes and therefore could play a role in the G0/G1 cell cycle transition. Defects in this gene are a cause of chromosome 9q subtelomeric deletion syndrome (9q-syndrome, also known as Kleefstra syndrome). Alternative splicing results in multiple transcript variants.
Versandbedingungen:
Blue Ice